A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217751



Internal ID20784791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:49913268..49913636hg38UCSC Ensembl
chr13:50487404..50487772hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg38369
hg19369
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582375
Supporting Variants
Samples
Known GenesSPRYD7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217751
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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